HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029040Generated: October 30, 2026
Potassium Hydroxide → HCID 53329886, compound
https://huagongshe.com/reaction/1029040
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Morpholineacetonitrile | HCID 22055 | — |
| Reactant | HCID 86676844 | HCID 86676844 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 53329886 | HCID 53329886 | — |
Reaction Steps
A solution of 2-morpholinoacetonitrile (37.7 mg, 0.299 mmol) in DMSO (0.5 mL) was treated with concentrated aqueous KOH (11M; 8.08 μL, 0.095 mmol). The reaction mixture was heated to 80° C. and a solution of N-(4′-amino-3′-formyl-6-methylbiphenyl-2-yl)-N,3,3-trimethylbutanamide (64 mg, 0.189 mmol) in DMSO (1 mL) was added dropwise. After 10 min the reaction mixture was diluted with water and aqueous saturated ammonium chloride solution. The aqueous mixture was extracted with DCM. The organic phase was separated and dried over MgSO4. The solvent was removed under reduced pressure and the remaining residue was purified by preparative HPLC (10-100% water with 0.1% TFA/CH3CN, 11 min). The titled compound was isolated as a light-yellow foam. MS (ESI, pos. ion) m/z: 447 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735384B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-87e90af8906d43dc80c0481480b91956 |
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| Source note | uspto-grants-2014_05 |
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